The management of secondary findings (SFs), which are beyond the intended purpose of the analysis, from clinical comprehensive genomic analysis using next generation sequencing (NGS) presents challenges. Policy statements regarding their clinical management have been announced in Japan and other countries. In Japan, however, the current status of and attitudes of clinical genetics professionals toward reporting them are unclear. We conducted a questionnaire survey of clinical genetics professionals at two time points (2013 and 2019) to determine the enforcement of the SF management policy in cases of comprehensive genetic analysis of intractable diseases and clinical cancer genome profiling testing. According to the survey findings, 40% and...
A follow-up nationwide survey on predictive genetic testing for late-onset neurological diseases in ...
HLA-VBSeq is an HLA calling tool developed to infer the most likely HLA types from high-throughput s...
Abstract Unprecedented progress in sequencing technolo-gies and decreasing cost have brought genomic...
Introduction: The rapid and growing integration of exome and genome sequencing into clinical genetic...
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
Comprehensive genomic profiling (CGP) testing by next-generation sequencing has been introduced into...
PurposeApproaches to secondary findings in genome sequencing (GS) are unresolved. In the United King...
With transformative initiatives like the UK’s 100,000 Genomes Project underway, vast amounts of data...
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
An increase in ethnic diversity in genetic studies has the potential to provide unprecedented insigh...
Background: Technological developments and discussions around autonomy and paternalism in clinical p...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Licen...
The aldehyde degrading function of the ALDH2 enzyme is impaired by Glu504Lys polymorphisms (rs671, t...
PURPOSE: Secondary findings (SFs) are present in 1-4% of individuals undergoing genome/exome sequenc...
A ψUSA300 clone of MRSA, a derivative of USA300, is uniquely found in Japan and has 12-bp deletion o...
A follow-up nationwide survey on predictive genetic testing for late-onset neurological diseases in ...
HLA-VBSeq is an HLA calling tool developed to infer the most likely HLA types from high-throughput s...
Abstract Unprecedented progress in sequencing technolo-gies and decreasing cost have brought genomic...
Introduction: The rapid and growing integration of exome and genome sequencing into clinical genetic...
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
Comprehensive genomic profiling (CGP) testing by next-generation sequencing has been introduced into...
PurposeApproaches to secondary findings in genome sequencing (GS) are unresolved. In the United King...
With transformative initiatives like the UK’s 100,000 Genomes Project underway, vast amounts of data...
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
An increase in ethnic diversity in genetic studies has the potential to provide unprecedented insigh...
Background: Technological developments and discussions around autonomy and paternalism in clinical p...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Licen...
The aldehyde degrading function of the ALDH2 enzyme is impaired by Glu504Lys polymorphisms (rs671, t...
PURPOSE: Secondary findings (SFs) are present in 1-4% of individuals undergoing genome/exome sequenc...
A ψUSA300 clone of MRSA, a derivative of USA300, is uniquely found in Japan and has 12-bp deletion o...
A follow-up nationwide survey on predictive genetic testing for late-onset neurological diseases in ...
HLA-VBSeq is an HLA calling tool developed to infer the most likely HLA types from high-throughput s...
Abstract Unprecedented progress in sequencing technolo-gies and decreasing cost have brought genomic...